A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148899



Internal ID21445676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142975287..142975594hg38UCSC Ensembl
chr8:144056704..144057011hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581917
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148899
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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